Autosomal Dominant Deafness 39 with Dentinogenesis Imperfecta 1
Autosomal Dominant Deafness 4
autosomal dominant nonsyndromic deafness 1
autosomal dominant nonsyndromic deafness 10
autosomal dominant nonsyndromic deafness 11
autosomal dominant nonsyndromic deafness 12
autosomal dominant nonsyndromic deafness 13
autosomal dominant nonsyndromic deafness 15
autosomal dominant nonsyndromic deafness 16
autosomal dominant nonsyndromic deafness 17
autosomal dominant nonsyndromic deafness 18
autosomal dominant nonsyndromic deafness 20
autosomal dominant nonsyndromic deafness 21
autosomal dominant nonsyndromic deafness 22
autosomal dominant nonsyndromic deafness 23
autosomal dominant nonsyndromic deafness 24
autosomal dominant nonsyndromic deafness 25
autosomal dominant nonsyndromic deafness 27
autosomal dominant nonsyndromic deafness 28
autosomal dominant nonsyndromic deafness 2A
autosomal dominant nonsyndromic deafness 2B
autosomal dominant nonsyndromic deafness 30
autosomal dominant nonsyndromic deafness 31
autosomal dominant nonsyndromic deafness 33
autosomal dominant nonsyndromic deafness 34
autosomal dominant nonsyndromic deafness 36
Autosomal Dominant Nonsyndromic Deafness 37
autosomal dominant nonsyndromic deafness 3A
autosomal dominant nonsyndromic deafness 3B
autosomal dominant nonsyndromic deafness 40
autosomal dominant nonsyndromic deafness 41
autosomal dominant nonsyndromic deafness 43
autosomal dominant nonsyndromic deafness 44
autosomal dominant nonsyndromic deafness 47
autosomal dominant nonsyndromic deafness 48
autosomal dominant nonsyndromic deafness 49
autosomal dominant nonsyndromic deafness 4A
autosomal dominant nonsyndromic deafness 4B
autosomal dominant nonsyndromic deafness 5
autosomal dominant nonsyndromic deafness 50
autosomal dominant nonsyndromic deafness 51
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has_material_basis_in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes. (DO)
autosomal dominant nonsyndromic deafness 52
autosomal dominant nonsyndromic deafness 53
autosomal dominant nonsyndromic deafness 54
autosomal dominant nonsyndromic deafness 56
autosomal dominant nonsyndromic deafness 58
autosomal dominant nonsyndromic deafness 59
autosomal dominant nonsyndromic deafness 6
autosomal dominant nonsyndromic deafness 64
autosomal dominant nonsyndromic deafness 65
autosomal dominant nonsyndromic deafness 66
autosomal dominant nonsyndromic deafness 67
autosomal dominant nonsyndromic deafness 68
autosomal dominant nonsyndromic deafness 69
autosomal dominant nonsyndromic deafness 7
autosomal dominant nonsyndromic deafness 70
autosomal dominant nonsyndromic deafness 71
autosomal dominant nonsyndromic deafness 72
autosomal dominant nonsyndromic deafness 73
autosomal dominant nonsyndromic deafness 74
autosomal dominant nonsyndromic deafness 75
autosomal dominant nonsyndromic deafness 76
autosomal dominant nonsyndromic deafness 77
autosomal dominant nonsyndromic deafness 78
autosomal dominant nonsyndromic deafness 79
Autosomal Dominant Nonsyndromic Deafness 80
Autosomal Dominant Nonsyndromic Deafness 81
Autosomal Dominant Nonsyndromic Deafness 82
Autosomal Dominant Nonsyndromic Deafness 83
Autosomal Dominant Nonsyndromic Deafness 84
Autosomal Dominant Nonsyndromic Deafness 85
Autosomal Dominant Nonsyndromic Deafness 86
Autosomal Dominant Nonsyndromic Deafness 87
Autosomal Dominant Nonsyndromic Deafness 88
Autosomal Dominant Nonsyndromic Deafness 89
autosomal dominant nonsyndromic deafness 9
Autosomal Dominant Nonsyndromic Deafness 90
Chromosome 10q Duplication Syndrome
chromosome 16p11.2 duplication syndrome
chromosome 16p13.3 duplication syndrome
Chromosome 16q12 Duplication Syndrome
chromosome 17p13.3 duplication syndrome
chromosome 17q12 duplication syndrome
chromosome 17q21.31 duplication syndrome
Chromosome 17q23.1-q23.2 Duplication Syndrome
chromosome 1p36.33 duplication syndrome
chromosome 1q21.1 duplication syndrome
chromosome 22q11.2 microduplication syndrome
chromosome 22q13 duplication syndrome
chromosome 2q31.1 duplication syndrome
chromosome 3q29 microduplication syndrome
chromosome 5p13 duplication syndrome
chromosome Xp11.22 duplication syndrome
chromosome Xp11.23-p11.22 duplication syndrome
Chromosome Xq13 Duplication Syndrome
Chromosome Xq26.3 Duplication Syndrome
Chromosome Xq27.3-q28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome
hereditary mixed polyposis syndrome 1
Klinefelter syndrome
NF1 Microduplication Syndrome
partial trisomy distal 4q
split hand-foot malformation 3
syndactyly type 1
syndromic X-linked intellectual disability Lubs type